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Biomedical subjects

Elizabeth M Hill

Publications and source records attributed to Elizabeth M Hill.

At least 19 recordsLinked to original sources

Moderated designs can balance between batch-effect mitigation and cell loss due to hashtag-assisted pooling in single-cell experiments.

Minimizing experimental noise is integral to robust data generation in single-cell omics. The current standard for avoiding batch effects during sample processing is barcode- or hashtag-assisted combining of different experimental treatments into one pool, allowing all samples to be subject to the technical protocols uniformly. The final data points for each treatment group are then computationally separated based on the original hashtag labels. Clearly, whereas hashtagging all groups and pooling them in a single well is expected to minimize batch effects, the procedure can also lead to a loss of cells that cannot be confidently decoded during the computational demultiplexing step. Here, we examine four alternate experimental designs, namely, compound, reference, chain, and confounded, that could be used instead of a single-pool approach and quantify the batch effects as well as cell loss in each case. We find a linear relationship-the percentage of cells lost is double the number of hashtags used in the experiment. We use these analyses to identify experimental designs that can successfully mitigate batch effects while minimizing multiplexing, hence the cell loss, in each well. Although a reference design offers the best overall performance, this study can help individual investigators choose particular approaches that are best suited for their biological questions.

Journal Article↗

CountASAP: a lightweight, easy to use python package for processing ASAPseq data.

BACKGROUND: Declining sequencing costs coupled with the increasing availability of easy-to-use kits for the isolation of DNA and RNA transcripts from single cells have driven a rapid proliferation of studies centered around genomic and transcriptomic data. Simultaneously, a wealth of new techniques have been developed that utilize single cell technologies to interrogate a broad range of cell-biological processes. One recently developed technique, transposase-accessible chromatin with sequencing (ATAC) with select antigen profiling by sequencing (ASAPseq), provides a combination of chromatin accessibility assessments with measurements of cell-surface marker expression levels. While software exists for the characterization of these datasets, there currently exists no tool explicitly designed to reformat ASAP surface marker FASTQ data into a count matrix which can then be used for these downstream analyses. RESULTS: To address this lack of a dedicated tool for ASAPseq data processing, we created CountASAP, an easy-to-use Python package purposefully designed to transform FASTQ files from ASAP experiments into count matrices compatible with commonly-used downstream bioinformatic analysis packages. CountASAP takes advantage of the independence of the relevant data structures to perform fully parallelized matches of each sequenced read to user-supplied input ASAP oligos and unique cell-identifier sequences. We directly compare the performance and user-friendliness of CountASAP to existing tools using similarly-structured data from a more common sequencing experiment: cellular indexing of transcriptomes and epitopes by sequencing (CITEseq). Further benchmarking against existing tools helps to identify proper defaults for CountASAP and assess the agreement of outputs from all tested software. A final test using a novel ASAPseq dataset provides evidence that CountASAP can generate biologically meaningful results that correlate well with paired chromatin accessibility data. CONCLUSIONS: CountASAP shows good agreement with existing, well-tested data processing tools in the analysis of similarly-structured benchmarking data. CountASAP runs efficiently on a standard laptop, has user-friendly documentation, a one-step installation, and represents the first and only tool designed specifically for the processing of ASAPseq data.

Software↗

Analysis of estrogens in river sediments by liquid chromatography-electrospray ionisation mass spectrometry. Comparison of tandem mass spectrometry and time-of-flight mass spectrometry.

A method has been developed and optimised for the determination of two natural estrogens, estrone (E1) and 17beta-estradiol (E2), and one synthetic estrogen, 17alpha-ethynylestradiol (EE2), in river sediments at the sub-ng/g level. This procedure includes microwave-assisted solvent extraction (MASE), solid-phase extraction and high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) with electrospray ionisation. Using sediments spiked with the three estrogens at 10 ng/g wet weight, efficient extraction (>92%) of all the three analytes was achieved by MASE, and whole-procedure recoveries ranged from 82 to 98%. Optimisation of the LC separation allowed for substantial reduction of ionisation suppression in the electrospray source to a final level of <18% suppression. Time-of-flight mass spectrometry (TOF-MS) and MS/MS were compared for the analysis of sediment extracts, with the latter technique proving to be the most selective. The method detection limits achieved by LC-MS/MS were 15, 30 and 40 pg/g for E1, E2 and EE2, respectively, which were 13-fold lower than those obtained by LC-TOF-MS. Analysis of river sediments collected from the River Ouse, UK, showed the presence of the natural estrogens at sub-ng/g level. E1 levels ranged from 0.40 ng/g (dry weight) to 3.30 ng/g while E2 levels ranged from <0.03 to 1.20 ng/g and EE2 was never detected (<0.04 ng/g).

Chromatography, Liquid↗

Identification of the steroid fatty acid ester conjugates formed in vivo in Mytilus edulis as a result of exposure to estrogens.

Vertebrate-type sex steroids have been detected in a number of mollusk species and may play a role in the reproductive physiology of the animal. Mollusks are also exposed to exogenous estrogenic steroids that are present in sewage effluents, and these may add to the estrogenic burden of exposed animals. We investigated the uptake of estrogens in the blue mussel, Mytlius edulis and report for the first time the identity of estrogen fatty acid ester metabolites formed in vivo in an invertebrate. We exposed mussels to waterborne radiolabeled [(14)C]-17beta-estradiol (E2) or estrone (E1) and determined the nature of their metabolites using radio-HPLC and mass spectrometry (MS). After 13 days of exposure to 10ng/L E2, concentrations of radiolabeled residues were 2428-fold higher in M. edulis soft tissues compared with the ambient water concentration of E2. All the E2 residues in the mussel were present as a lipophilic ester which, in depuration studies, had a half-life of 8.3 days. Exposure of mussels to [(14)C]-E1 (70ng/L) resulted in formation of a similar lipophilic metabolite that after hydrolysis released [(14)C]-E2. Tandem MSMS analyses of the purified steroid ester fraction isolated from mussels exposed to either E2 or E1 revealed that they had the same composition and comprised C16:0, C16:1 and C16:2 esters of E2. This work reveals that in vivo E1 is rapidly metabolized to E2 in mussels prior to conjugation to C16 fatty acid esters, proving that C17-ketoreductase and C16 fatty acid acyl-CoA:E2 acyltransferase are important enzymes for the metabolism of estrogens in M. edulis.

Animals↗

Identification and steroid receptor activity of products formed from the bromination of technical nonylphenol.

Alkylphenols are commonly present in wastewater effluents and may contribute to the total hormonal loading of receiving waters due to their weakly estrogenic properties. However the presence of reactive bromine species in some treated wastewaters can result in the formation of brominated alkylphenols which may also possess steroid receptor activity. In this study, the products of bromination of technical nonylphenol (NP) were identified, purified and tested in vitro in recombinant yeast steroid receptor transcription assays. Bromination of NP in the presence of acetic acid resulted in the formation of one major product which was identified as 2-bromo-4-nonylphenol (NPBr). In the presence of methanol/water, bromination of NP resulted in the formation 2,6-dibromo-4-nonylphenol (NPBr2) as well as a number of other minor polybrominated products. The EC50 of NPBr in the yeast estrogen receptor transcription (YES) assay was 6.7x10(-6) M, which was 48 fold less active than NP and 86,000 fold less active than the estrogen agonist 17beta-estradiol NPBr2 was not active in the YES assay. NP, NPBr and NPBr2 were all weakly androgenic in the yeast androgen receptor transcription assay but at concentrations which were 100,000 fold less active than the androgen receptor agonist dihydrotestosterone. Neither NP, NPBr or NPBr2 exhibited appreciable anti-estrogenic or anti-androgenic activity in the yeast receptor transcription assays. This study suggests that bromination of NP markedly reduces its estrogen receptor transcription activity but has no effect on the weak androgen receptor transcription activity of the alkylphenol.

Bromine↗

Profiles of short chain oligomers in roach (Rutilus rutilus) exposed to waterborne polyethoxylated nonylphenols.

Nonylphenol polyethoxylates (NPEOs) are common contaminants in the aquatic environment through their use as industrial surfactants and their discharge in wastewaters and effluents. In order to assess the bioavailability of NPEOs to fish, we studied the fate of two different oligomeric mixtures of NPEOs in adult roach Rutilus rutilus. Fish were exposed to [14C] radiolabelled NPEOs, averaging either 3 ethoxy units (NP(3av)EO) or 7 ethoxy units (NP(7av)EO), over a 4-day period in a flow-through aquarium. A method was developed to extract radioactive residues from soft tissues and analyse their composition by normal phase radio-HPLC and GC-MS. Radioactive residues were detected in all soft tissues of the roach dosed with either of the test mixtures, but the concentration of NPEO residues in each tissue were highest in fish exposed to the NP(3av)EO compared with the NP(7av)EO test mixture. Radioactive concentrations in roach dosed with 14C NP(3av)EO were highest in the bile at a mean concentration+/-S.E. of 62+/-3 microg/g wet weight, whereas concentrations in the liver, kidney and brain tissues ranged between 1 and 2 microg/g and concentrations in other soft tissues were between 0.1 and 0.7 microg/g. Analysis of the radioactive residues in bile of roach exposed to the NPEO test mixtures indicated that they were mainly metabolites including glucuronide conjugates, whereas in muscle, ovary and gill tissues they were a mixture of NP and short chain NPEO oligomers comprising 1-4 ethoxy units. This study suggests that short chain NPEO oligomers are taken up via the gills and accumulate in tissues such as gonads which are sensitive to endocrine disruption, whereas waterborne NPEOs containing more than 4 ethoxymers are not bioavailable to roach.

Animals↗

Uptake and metabolism of technical nonylphenol and its brominated analogues in the roach (Rutilus rutilus).

Alkylphenols have been implicated as one of the causative agents of oestrogenic contamination in fish. This study reports the fate of a technical mixture of secondary and tertiary isomers of the environmental contaminant 4-nonylphenol (NP) in mature female roach. Fish were exposed to a concentration of 4.9microg/l radio-labelled technical NP over a 4-day period in a flow-through aquarium. NP residues were extracted from all tissues and analysed by reverse phase radio HPLC. The concentration of NP residues was highest in bile and liver, with apparent bioconcentration factors (apparent BCFs) of 34,121 and 605, respectively. In other tissues, apparent BCF values were recorded between 13 and 250. NP was the only residue detected in brain, muscle and blood cells whereas an additional NP derivative was detected in other soft tissues, including gonads and liver, which was identified as the brominated derivative of technical NP, dibromo-4-nonylphenol. Traces of the dibrominated NP were also detected in aquarium water but only in the presence of NP, which suggested that bromination of the NP parent compound occurred in situ in the water due to the presence of trace amounts of oxidised bromine species in municipal water following disinfection. There was no evidence of further metabolism of the brominated derivative in roach, but a single major metabolite of NP was present in liver and bile, which was identified as the glucuronide conjugate of 4-(hydroxy-nonyl)-phenol. This detection of only one NP metabolite suggests that, in contrast to other fish species, the variety of metabolic pathways available for the deactivation of 4-alkylphenols in roach is limited. This study indicates that brominated alkylphenols bioconcentrate in a range of tissues and, as they have been detected in the aquatic environment, they could contribute to the body burden of alkylphenolics in fish. The formation of these brominated derivatives in aquarium water suggest that they could confound toxicity tests to assess the effects of alkyphenols to aquatic organisms.

Animals↗

Camp health services in the state of Michigan.

CONTEXT: Every summer, 10 million campers attend summer camp in the United States. In Michigan, each camp is required to have a camp health officer (CHO) on-site. OBJECTIVE: To document the medical training, local emergency medical services and physician support, and off-camp medical facility use of CHOs. DESIGN: Anonymous institutional review board-approved mail survey of all Michigan CHOs during the summer of 2001. RESULTS: A total of 129 responses (50% response rate). Forty-seven percent of the CHOs reported caring for campers with significant medical needs. Almost half (45%) of the CHOs were registered nurses; however, 44% of the CHOs had paramedic training or less. Forty percent reported an ambulance response time of more than 10 minutes. Nearly all (97%) reported having a physician who reviewed their standing orders, and yet 75% reported using an acute care facility (emergency department or urgent care) more than half of the time for medical care not on-site. The CHOs reported that a small or rural hospital was the ambulance-receiving hospital 71% of the time. Two of the camps that responded have an automatic external defibrillator, and 22% are planning to buy one. CONCLUSIONS: In Michigan, CHOs have limited training, tend to use emergency department or urgent care facilities as their medical backup, and, in some instances, have prolonged times to definitive care. This preliminary study shows some of the opportunities that exist to improve health care for campers on a local and national level.

Adolescent↗

Sediments are major sinks of steroidal estrogens in two United Kingdom rivers.

The occurrence of intersex fish in a number of European rivers has been attributed to exposure to estrogenic chemicals present in sewage treatment work (STW) effluents. To further understand the environmental fate of these contaminants, the estrogenic activity of effluents, water, and sediments were investigated both upstream and downstream of the major STW discharge in two United Kingdom rivers. Estrogenic activity, determined using the yeast estrogen-receptor transcription screen, of the major STW effluents on both rivers was similar, ranging from 1.4 to 2.9 ng 17beta-estradiol equivalents (EEQ)/L. Estrogenic activities of surface waters 1 km upstream and downstream of both STW inputs were less than the limits of detection (0.04 ng/L); however, levels of estrogenic activity in sediments were between 21.3 and 29.9 ng EEQ/kg and were similar at both upstream and downstream sites. Effluent and sediment extracts were fractionated by reverse phase-high-performance liquid chromatography, and estrogenic active fractions were further analyzed by gas chromatography-mass spectrometry. The major active chemicals in the two effluents and in the sediments were estrone with lesser amounts of 17beta-estradiol; however, at one site, a number of other unidentified estrogenic fractions were detected in the sediments. These results suggest that riverine sediments are a major sink and a potential source of persistent estrogenic contaminants.

Animals↗

Comparing alcoholic and nonalcoholic parents on the family unpredictability scale.

Research findings and clinical observations suggest that families with an alcoholic parent are more unpredictable. Alcoholic parents (n=25, 68% men, 68% Euro-American, M age=38.6 yr.) and community parents (n=27, 52% men, 70% Euro-American, M age=38.8 yr.) completed the self-report Family Unpredictability Scale of Ross and Hill. Alcoholic parents reported significantly higher (less predictability) scores on the subscales of Nurturance, Finances, and Discipline, as well as on the Total Family Unpredictability Scale (ps<.01). This appears to be the first study on family unpredictability and parental alcoholism in which parental reports of multiple dimensions of unpredictability are used. We provide suggestions for research and clinical uses of the scale, especially pertaining to families with an alcoholic parent.

Adult↗

Impairment in family caregiving: a biological perspective.

This paper focuses on patterns in the care of children and dependent elders, providing a new perspective to understand impairment in family caregiving. One concept from evolutionary theory, kin selection, has promise for providing a broad framework for understanding patterns of family caregiving. We present an application of the evolutionary model to the issue of family care decisions in the face of potential conflicts of interest. Specifically, a mathematical biological model, which was developed to understand self-preservation motivation, is applied to the kin investment decision. Using the evolutionary model, the main predictors of investment would be relatedness, reproductive value, and expected benefit from the care invested. The biological model accounts very simply for decisions between caring for an elder parent or caring for your own child, and for decisions by two daughters (one with a child, one childless) to care for an elder parent. The factors that form the basis of an evolutionary model (relatedness, reproductive value, and benefit from care) have not been widely investigated in family care studies, however, and this absence reveals new directions for future research.

Aged↗

Alcohol effects on motor vehicle crash injury.

CONTEXT: Although alcohol is frequently present in injured patients, whether it exacerbates injury and whether tolerance to alcohol changes such a relationship is less clear. Most clinical studies do not consider other important predictors of injury, making interpretation of their findings problematic. OBJECTIVE: To examine alcohol's role in injuries, taking into account other important factors, and to examine the effect of tolerance, if any. DESIGN: Prospective cohort study. SETTING: University hospital and community hospital emergency departments and morgue. PATIENTS: 1362 Motor Vehicle Crash patients age >/=18, treated and released, admitted, and deceased. MAIN OUTCOME MEASURES: Excess injury measured by Injury Severity Scale (ISS) 90, Weighted Revised Trauma Score (WRTS), and G-Score. RESULTS: Using regression analysis, the best predictors of injury severity were vehicle crush (TAD), safety belt use, and their interaction, and age. Alcohol use further predicted injury. Using the final regression model, the effect of alcohol was to increase ISS90, on average, by about 30% (from a predicted ISS90 of 5.1 to 6.8, all else being equal). The adjusted odds ratio for serious injury (ISS90>15), was 1.59 for a patient with a positive blood alcohol concentration (alc+) compared to a alc- patient. This potentiating effect is seen even for patients with low levels of alcohol (<22 mmol/liter; <0.100 BAC) but is not linear with increasing alcohol level. Tolerance to alcohol did not affect the potentiation of injury by alcohol. CONCLUSION: When other relevant variables are considered, alcohol increases injury, but the effects of alcohol level and alcohol tolerance are less clear. These findings have important implications for injury prevention, treatment, and research.

Accidents, Traffic↗

Tissue distribution and depuration of 4-tert-octylphenol residues in the cyprinid fish, Scardinius erythrophthalmus.

Alkylphenols are present in the aquatic environment through the degradation of alkylphenolpolyethoxylate surfactants in sewage treatment works. Branched chain 4-alkylphenols have been shown to retard testicular growth and stimulate vitellogenin synthesis in freshwater fish. We conducted in vivo studies in order to determine the fate and persistence of radiolabeled 4-tert-octylphenol (tOP) in the cyprinid fish, rudd (Scardinius erythrophthalmus). Sexually mature rudd were exposed to a concentration of 4.7 microg/L of [14C] tOP in a flow through system for 10 days. Radioactive residues were extracted from soft tissues and analyzed by radio-high-performance liquid chromatography. tOP accumulated as the major residue in muscle, ovary, and testis with bioconcentration factors of 24, 85, and 169, respectively. tOP residues in blood, gill, kidney, liver, and bile were extensively metabolized. Analysis of tOP residues in bile revealed 10 major metabolites, which were identified by GC-MS as products of aromatic and aliphatic hydroxylation, glucuronidation, and glucosidation. Depuration studies with exposed fish placed in clean water for up to 10 days resulted in a rapid loss of soluble residues from the tissues with half-lives of between 0.7 and 1.0 days (muscle, testis, ovary, gill, blood, kidney), 1.7 days (liver), and 5.9 days (bile). A further portion of radioactive residues was extracted from blood, gill, kidney, and liver after alkaline digestion, suggesting the formation of covalently bound protein adducts in these tissues. This study suggests that although para-alkyphenolic xenoestrogens can accumulate in muscle and the gonads of adult fish, residues are rapidly depurated from these tissues. Furthermore, analysis of the parent alkylphenol in bile, after hydrolysis of the conjugates, is likely to significantly underestimate the total concentration of alkylphenol residues and may not serve as an appropriate biomarker for quantifying the exposure of wild fish to alkylphenols.

Animals↗

Life-history theory and risky drinking.

AIMS: Life-history theory, a major theory related to evolutionary biology and behavioral ecology, is applied to analyze patterns in alcohol abuse and dependence. The life-history approach examines how intensity of reproductive competition affects the benefits and costs of risk-taking, which are typically greater for young men than for women or older men. We used this framework to predict demographic variation in hazardous patterns of alcohol use, assuming that they reflect risk-taking in general. DESIGN: This paper is a review of literature on demographic patterns in risky drinking and alcohol dependence. Predictions are generated using evolutionary analysis of risk-taking. Existing surveys of drinking behavior are reviewed, and findings are compared to predictions. FINDINGS: Results were generally consistent with predictions. The frequency of risky drinking and dependence is higher for men, and people of younger age, single marital status, childless parental status or unstable environmental resources. An exception is the effect of educational attainment. which is inconsistent. CONCLUSIONS: Risky drinking behavior, as with other forms of physical risk-taking, is more frequently observed in young men, and it increases where environmental instability is higher. The utility of life-history theory is compared to alternate conceptions of risky drinking and dependence. Implications of this perspective for research and clinical efforts are explored.

Adolescent↗

Prevalence of domestic violence and associated factors among women on a trauma service.

BACKGROUND: Despite the increasing recognition of the problem of domestic violence (DV), it has not been studied in surgical populations. METHODS: Eligible patients underwent screening for a recent history of DV and alcohol abuse (AA). Other demographic, health, and injury-related data were also collected. RESULTS: Of 127 subjects entered into the study, 18% screened positive for DV and 21% screened positive for AA. Of those screening positive for DV, 65% screened positive for AA compared with 12% of those screening negative for DV (p < 0.001.) Screening for DV was recommended by a vast majority of subjects, with only 6% of subjects responding that it was not appropriate. CONCLUSION: Both DV and AA have a high prevalence among female trauma patients admitted to trauma centers. Nearly all subjects recommended screening for DV. Screening for DV should be incorporated into the routine care of female trauma patients.

Adult↗

Antisocial alcoholism and serotonin-related polymorphisms: association tests.

Central serotonin dysfunction appears to be related to a subtype of alcoholism with antisocial impulsive features (type II; antisocial alcoholism). The serotonergic deficit may be associated with greater impulsivity, which in turn facilitates both alcohol dependence and antisocial behavior. The present study tested association of antisocial impulsive alcoholism with candidate genes related to serotonergic neurotransmission, using families. Eight markers were assayed using polymerase chain reaction: tryptophan hydroxylase (intron 7), the serotonin transporter SLC6A4 (VNTR 9/12), HTTLPR, the three serotonin receptor types HTR1B (G861C), HTR2A (T102C) and HTR2C (Cys23Ser), monoamine oxidase A (T1460C), and (CA)(n). Eligible probands had early age of onset of alcoholism, child conduct disorder, and two or more symptoms of adult Antisocial Personality Disorder. This sample included 35 probands, their parents, and some siblings (n = 116). Association tests were conducted using the Haplotype Relative Risk method for antisocial alcoholism diagnosis and the George-Elston regression method (the S.A.G.E. program ASSOC) for quantitative antisocial alcoholism severity. Haplotype Relative Risk analyses were not significant at the 0.05 level for any of the markers. Trends suggestive for future research occurred for tryptophan hydroxylase and HTR2A. Quantitative ASSOC analyses showed significant marker effects (P < 0.05) for both monoamine oxidase A markers, which were in linkage disequilibrium. Antisocial alcoholism symptom severity was higher with monoamine oxidase A C homozygotes or hemizygotes, indicating that low monoamine oxidase activity may be important. Future studies are needed to examine joint and interactive effects of serotonin-related markers.

Adult↗